Gallo P, Formigari R, Hokayem N J, D'Offizi F, Francalanci P, d'Amati G, Colloridi V, Pizzuto F
Department of Human Biopathology, La Sapienza University, Rome, Italy.
Clin Cardiol. 1991 Jun;14(6):513-21. doi: 10.1002/clc.4960140611.
Subaortic stenosis has been described with increasing frequency as an ominous feature of atrioventricular septal defect (AVSD), especially following surgical correction of the anomaly in non-Down's syndrome patients. In order to study the surgical anatomy of the left ventricular outflow tract in this malformation, 48 hearts featuring AVSD were examined. Obstructive lesions were classified into unequivocal forms (class A, 13.5%) and potential ones (class B, 10.8%). In the remaining hearts (class C, 75.7%) no obstruction was noted. In class A, subaortic stenosis was due to exaggeration of the anticipated anomalous arrangement of atrioventricular valve tensor apparatus, to the persistence of a subaortic muscular infundibulum, and to a discrete fibrous diaphragm. A potential for subaortic stenosis is provided by the unwedged position of the aortic valve. The left ventricular outflow tract is transformed into a long, forward-displaced fibromuscular channel. Morphometric analysis showed in AVSD (with both common annulus and separate orifices) a significantly (p less than 0.01) lower inflow/outflow tract ratio, and a significantly (p less than 0.01) lower right ventricular/left ventricular outflow length ratio than normal hearts. These results suggest that AVSD is characterized not only, as commonly stated, by inflow tract shortening, but by outflow tract lengthening as well. On these anatomical grounds, nearly all cases of AVSD could harbor the potential for subaortic stenosis; however, this becomes a real hazard (class B) only when associated with forward displacement of the left anterior papillary muscle, or direct insertion on the ventricular septum of the anterior bridging leaflet, and it may be converted to an actual obstruction by the effects of surgery.(ABSTRACT TRUNCATED AT 250 WORDS)
主动脉瓣下狭窄作为房室间隔缺损(AVSD)的一个不祥特征,其报道频率日益增加,尤其是在非唐氏综合征患者的该畸形手术矫正之后。为了研究这种畸形中左心室流出道的手术解剖结构,对48例患有AVSD的心脏进行了检查。梗阻性病变分为明确型(A类,13.5%)和潜在型(B类,10.8%)。在其余心脏(C类,75.7%)中未发现梗阻。在A类中,主动脉瓣下狭窄是由于房室瓣张量装置预期异常排列的过度、主动脉瓣下肌性漏斗的持续存在以及一个离散的纤维隔膜所致。主动脉瓣的未楔入位置提供了主动脉瓣下狭窄的可能性。左心室流出道转变为一个长的、向前移位的纤维肌性通道。形态计量分析显示,在AVSD(既有共同瓣环又有分开的瓣口)中,流入道/流出道比值显著(p<0.01)低于正常心脏,右心室/左心室流出道长度比值也显著(p<0.01)低于正常心脏。这些结果表明,AVSD不仅如通常所说的以流入道缩短为特征,而且还以流出道延长为特征。基于这些解剖学依据,几乎所有AVSD病例都可能存在主动脉瓣下狭窄的可能性;然而,只有当与左前乳头肌向前移位或前桥瓣叶直接插入室间隔相关时,这才会成为真正的危险因素(B类),并且它可能因手术影响而转变为实际梗阻。(摘要截断于250字)